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异位皮质醇分泌腺瘤和腹膜后神经鞘瘤并存,罕见病例报告
Authors Shi L , Hu J, Xu X, Wang Y, Xu S, Tu L
Received 17 July 2024
Accepted for publication 23 November 2024
Published 28 November 2024 Volume 2024:17 Pages 4565—4570
DOI https://doi.org/10.2147/DMSO.S487334
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Prof. Dr. Juei-Tang Cheng
Lingfeng Shi,1 Jiongyu Hu,1 Xiaoli Xu,2 Yongquan Wang,3 Senlin Xu,4 Lijuan Tu2
1Endocrinology Department, First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, People’s Republic of China; 2Third Military Medical University (Army Medical University), Chongqing, People’s Republic of China; 3Urology Department, First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, People’s Republic of China; 4Pathology Department, First Affiliated Hospital of Third Military Medical University (Army Medical University), Chongqing, People’s Republic of China
Correspondence: Lijuan Tu, Email 251881081@qq.com
Background: Ectopic cortisol-producing adrenocortical adenoma (ECPA) is extremely rare, with only a few cases reported. Retroperitoneal schwannoma is also uncommon, accounting for only 0.7– 5% of all schwannomas. It is peculiar to have both conditions at the same time, and it is intriguing to explore their possible connection. Herein, we present a case of both ECPA and retroperitoneal schwannoma and provide our conjectures regarding their co-occurrence.
Case Presentation: A 38-year-old female presented with a two-year history of facial and lower limb edema, as well as chest tightness and palpitations for the past four months. Physical examination revealed hypertension, a high body mass index (BMI), moon face, thick neck and back fat, abdominal obesity, and purple striae on the abdomen. Laboratory tests indicated an persistent increased cortisol level and suppression of adrenocorticotropic hormone (ACTH). Adrenal-enhanced computed tomography (CT) scan showed that both adrenal glands appeared normal without evident adenomas or hyperplasia. However, the scan revealed two lesions located in the right renal hilum and retroperitoneal area positioned anteriorly to the lower margin of the lumbar 2 pyramid. Further imaging using 68Ga-DOTATATE PET/CT revealed concentrated radiotracer uptake in the tumor at the right renal hilum, indicating it may be responsible for the patient’s Cushing’s symptoms. After laparoscopic resection of these masses, clinical symptoms improved significantly. Postoperative pathology confirmed the right renal hilum one lesion as an ECPA while identifying another lesion as a schwannoma.
Conclusion: Our literature reported a case with the diagnosis of both ECPA in the right renal hilum and retroperitoneal schwannoma. 68Ga-DOTATATE PET/CT imaging can provide functional and locational information on tumors, enabling a comprehensive examination of the entire body to identify lesions that require appropriate treatment.
Keywords: ectopic adrenocortical adenoma, schwannoma, cortisol-producing adrenocortical adenomas, Cushing syndrome, case report